Author(s): RubioCamarillo M, GmezLpez G, Fernndez JM, Valencia A, Pisano DG
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Abstract MOTIVATION: RUbioSeq has been developed to facilitate the primary and secondary analysis of re-sequencing projects by providing an integrated software suite of parallelized pipelines to detect exome variants (single-nucleotide variants and copy number variations) and to perform bisulfite-seq analyses automatically. RUbioSeq's variant analysis results have been already validated and published. AVAILABILITY: http://rubioseq.sourceforge.net/.
This article was published in Bioinformatics
and referenced in Journal of Bioequivalence & Bioavailability